Canonical Allele Identifier: PA645421433
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356398
ClinVar RCV Id: RCV000290480 RCV000344614 RCV000379273 RCV000400234 RCV001538789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Gly895Ala
CA3750764
NM_080680.3:c.2684G>C